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MANI Disposable Vessel Knife - Indonesia BPOM Medical Device Registration

MANI Disposable Vessel Knife is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10504022794. The device is manufactured by MANI HANOI CO., LTD, PHO YEN FACTORY from Vietnam, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is OPHTHALINDO JAYA.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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BPOM Registered
Risk Class Kelas Resiko : A
MANI Disposable Vessel Knife
Analysis ID: AKL 10504022794

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Vietnam

Authorized Representative

OPHTHALINDO JAYA

AR Address

KOMPLEK KEMAYORAN MEGA GLODOK, BLOK A NO.8, GUNUNG SEHARI SELATAN

Registration Date

May 19, 2020

Expiry Date

Dec 31, 2023

Product Type

Surgical Cardiology Equipment

Cardiovascular surgical instruments.

Non Electromedic Sterile

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